This study is currently recruiting participants.
Number
13-CC-0099
Sponsoring Institute
National Institutes of Health Clinical Center (CC)
Recruitment Detail
Type: Participants currently recruited/enrolled Gender: Male & Female Min Age: 18 Years Max Age: 55 Years
Referral Letter Required
No
Population Exclusion(s)
Children;Pregnant Women;Fetuses
Keywords
Muscle Force; Knee; Magnetic Resonance Imaging; Quadriceps; Ultrasound; Natural History
Recruitment Keyword(s)
None
Condition(s)
Patellofemoral Pain Syndrome
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Supporting Site
NIH Clinical Center
- Researchers are interested in how the muscles affect the movement of the knee cap. These muscles may be related to different kinds of knee pain that are not caused by an injury or a disease. Imaging studies such as magnetic resonance imaging (MRI) can be used to look at these muscles. To study these muscles and how they move, researchers will use MRI to look at healthy individuals and individuals with knee cap pain.
Objectives:
- To study how changes to the muscles around the knee can influence knee pain.
Eligibility:
- Individuals between 18 to 55 years of age who have knee cap pain that cannot be explained by a specific injury or disease.
- Healthy volunteers between 18 and 55 years of age.
Design:
- Participants will be screened with a physical exam and medical history.
- This study requires two visits. Each visit will use standard MRI sequences to take images of the knee in motion and at rest.
- On the first visit, the MRI scan will look at the knee in its natural state. Participants will move the knee up and down for 1 to 3 minutes at a time during the scan.
- On the second visit, a local anesthetic agent will be injected into the muscle of the thigh. The anesthetic will block this muscle from generating force for 2 or 3 hours. Participants will move the knee up and down for 1 to 3 minutes at a time during the MRI scan.
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INCLUSION CRITERIA: 1) Male and female volunteers between the ages of 18 and 55 EXCLUSION CRITERIA: All Volunteers 1) Any relevant medical problems, including 933 those preventing ambulation 2) Any serious injury to the joint being studied, previous surgery on the joint being studiedor extreme pain at the joint being studied or other condition that may explain the presence of PF_pain (e.g., meniscal tear, arthritis) 3) Allergy/hypersensitivity to any local anesthetic agent (e.g., Novocain, lidocaine, bupivacaine, ropivacaine) 4) Liver disease 5) Open angle glaucoma 6) Cardiac arrhythmias, congenital heart disease 7) Glucose-6-phosphate dehydrogenase deficiency 8) Any female who is pregnant A volunteer will be excluded if they have a contraindication to MR imaging. Examples are: 1) Metal within their body, which might be expected to concentrate radiofrequency fields or cause tissue damage from twisting in a magnetic field (e.g., aneurysm clip, implanted neural stimulator, implanted cardiac pacemaker or autodefibrillator, cochlear implant, other foreign body (e.g. metal shavings, insulin pump). 2) A condition, which would preclude them from participating in an MR imaging study (e.g., paralyzed hemidiaphragm, morbid obesity, severe claustrophobia) 3) A condition that presents an unnecessary risk to them or their unborn child (e.g., 953 pregnancy, previous surgery of uncertain type, symptoms of pheochromocytoma or insulinoma) Subjects with Chronic Idiopathic Patellofemoral Pai: 1. Lack of PF_pain (either no active pain or current pain of < 6 months duration) Control Volunteers: 1. Any clinical signs of a knee impairment in the joint being studied, including abnormal range of motion, muscle weakness, malalignment, and ligament damage. 2. The presence of PF_pain (either active or past)
1) Male and female volunteers between the ages of 18 and 55
EXCLUSION CRITERIA:
All Volunteers
1) Any relevant medical problems, including 933 those preventing ambulation
2) Any serious injury to the joint being studied, previous surgery on the joint being studiedor extreme pain at the joint being studied or other condition that may explain the presence of PF_pain (e.g., meniscal tear, arthritis)
3) Allergy/hypersensitivity to any local anesthetic agent (e.g., Novocain, lidocaine, bupivacaine, ropivacaine)
4) Liver disease
5) Open angle glaucoma
6) Cardiac arrhythmias, congenital heart disease
7) Glucose-6-phosphate dehydrogenase deficiency
8) Any female who is pregnant
A volunteer will be excluded if they have a contraindication to MR imaging. Examples are:
1) Metal within their body, which might be expected to concentrate radiofrequency fields or cause tissue damage from twisting in a magnetic field (e.g., aneurysm clip, implanted neural stimulator, implanted cardiac pacemaker or autodefibrillator, cochlear implant, other foreign body (e.g. metal shavings, insulin pump).
2) A condition, which would preclude them from participating in an MR imaging study (e.g., paralyzed hemidiaphragm, morbid obesity, severe claustrophobia)
3) A condition that presents an unnecessary risk to them or their unborn child (e.g., 953 pregnancy, previous surgery of uncertain type, symptoms of pheochromocytoma or insulinoma)
Subjects with Chronic Idiopathic Patellofemoral Pai:
1. Lack of PF_pain (either no active pain or current pain of < 6 months duration)
Control Volunteers:
1. Any clinical signs of a knee impairment in the joint being studied, including abnormal range of motion, muscle weakness, malalignment, and ligament damage.
2. The presence of PF_pain (either active or past)
Principal Investigator
Referral Contact
For more information: